Colon Cancer: Gene >> TPPP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290942
Start	67390229:67390229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476G>A
AA Mutation	p.Gly159Asp(p.G159D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290942
Start	67390236:67390236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Asp157Asn(p.D157N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290942
Start	67390293:67390293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562124643
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Cys(p.R138C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290942
Start	67390309:67390309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768698901
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290942
Start	67390353:67390353(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.352delA
AA Mutation	p.Thr118GlnfsTer5(p.T118Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TPPP3

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290942
Start	67391049:67391050(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.62_63insATGGCTGGGCTGGAGGAGAGCTTCCGCAAGTTTGTCATCCATGG
AA Mutation	p.Asp22TrpfsTer24(p.D22Wfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript